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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7071269inversion1nstd229human GRCh38 chr20: 51,579,374-58,024,568 , GRCh37.p13 chr20: 50,195,913-56,599,624 CBLN4, LOC105372693, 89 more genes
    nsv7066855inversion1nstd229human GRCh38 chr20: 57,440,795-58,210,449 , GRCh37.p13 chr20: 56,015,851-56,785,505 LINC01742, LOC105372692, 13 more genes
    nsv7063616inversion1nstd229human GRCh38 chr20: 51,911,434-57,961,609 , GRCh37.p13 chr20: 50,527,973-56,536,665 FAM210B, BCAS1, 81 more genes
    nsv7058267inversion1nstd229human GRCh38 chr20: 51,559,821-57,992,303 , GRCh37.p13 chr20: 50,176,360-56,567,359 LOC105372683, MRPS33P4, 89 more genes
    nsv7037339copy number variation1nstd229human GRCh38 chr20: 57,325,590-57,659,163 , GRCh37.p13 chr20: 55,900,646-56,234,219 CTCFL, HMGB1P1, 13 more genes
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7024807copy number variation1nstd229human GRCh38 chr20: 56,642,648-58,322,378 , GRCh37.p13 chr20: 55,217,704-56,897,434 MIR4325, LOC105372693, 36 more genes
    nsv7018337copy number variation1nstd229human GRCh38 chr20: 57,534,757-58,246,724 , GRCh37.p13 chr20: 56,109,813-56,821,780 CIMIP1, NKILA, 12 more genes
    nsv6314094copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,292,205-57,866,365 , GRCh38.p12 chr20: 56,717,149-59,291,310 PCK1, MIR296, 58 more genes
    nsv6311086copy number variation1nstd102humanUncertain significance GRCh37 chr20: 54,823,900-57,899,514 , GRCh38.p12 chr20: 56,248,844-59,324,459 CTSZ, SPO11, 75 more genes
    nsv6134308copy number variation1nstd213human GRCh37 chr20: 55,660,000-60,880,001 , GRCh38.p12 chr20: 57,084,944-62,304,945 TAF4, OSBPL2, 97 more genes
    nsv6134040copy number variation1nstd213human GRCh37 chr20: 51,820,000-60,870,001 , GRCh38.p12 chr20: 53,203,461-62,294,945 MC3R, PPP1R3D, 142 more genes
    nsv6133831copy number variation1nstd213human GRCh37 chr20: 54,010,000-57,120,001 , GRCh38.p12 chr20: 55,393,462-58,544,945 BMP7, SPO11, 62 more genes
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5178576mobile element insertion1nstd203human GRCh38 chr20: 57,563,859-57,563,875 , GRCh37.p13 chr20: 56,138,915-56,138,931 PCK1
    nsv4678958copy number variation1nstd189human GRCh37.p13 chr20: 55,665,635-56,143,223 , GRCh38.p12 chr20: 57,090,579-57,568,167 BMP7, PCK1, 17 more genes
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4507915mobile element insertion1nstd166human GRCh37.p13 chr20: 56,138,915-56,138,915 , GRCh38.p12 chr20: 57,563,859-57,563,859 PCK1
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
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